TY - JOUR
T1 - The role of dendritic cells in multiple sclerosis
AU - Wu, Gregory F.
AU - Laufer, Terri M.
N1 - Funding Information:
GFW is supported by a post-doctoral fellowship from the National Multiple Sclerosis Society. TML is supported by a pilot research award from the National Multiple Sclerosis Society. We would like to thank Eric J. Allenspach for critical reading of the manuscript.
PY - 2007/5
Y1 - 2007/5
N2 - Although multiple sclerosis (MS) is a presumed T-cell-mediated disease, it is unclear what triggers the development of neuroantigen-specific T cells. Autoreactive CD4+ T cells are activated by antigen presenting cells; dendritic cells (DCs) are the primary antigen presenting cells directing T-cell functions and are, therefore, extremely important in directing the immune pathology characteristic of MS. Three important concepts have emerged regarding DCs in MS. First, DCs are present within the healthy central nervous system (CNS) in association with the cerebrospinal fluid space and micro-vasculature. Therefore, the potential for sampling of CNS antigens in similar fashion to other tissues and organs exists and likely plays an integral role in CNS immunity. The degree of involvement, as well as the source, of these CNS DCs has been addressed by several studies using the experimental autoimmune encephalomyelitis animal model. Second, DCs are found within MS lesions and have been shown to be functionally abnormal in patients with MS. Lastly, therapeutics directed at DCs could potentially be engineered for treatment in MS and in fact may already be involved in the mechanisms of current immunomodulatory therapies.
AB - Although multiple sclerosis (MS) is a presumed T-cell-mediated disease, it is unclear what triggers the development of neuroantigen-specific T cells. Autoreactive CD4+ T cells are activated by antigen presenting cells; dendritic cells (DCs) are the primary antigen presenting cells directing T-cell functions and are, therefore, extremely important in directing the immune pathology characteristic of MS. Three important concepts have emerged regarding DCs in MS. First, DCs are present within the healthy central nervous system (CNS) in association with the cerebrospinal fluid space and micro-vasculature. Therefore, the potential for sampling of CNS antigens in similar fashion to other tissues and organs exists and likely plays an integral role in CNS immunity. The degree of involvement, as well as the source, of these CNS DCs has been addressed by several studies using the experimental autoimmune encephalomyelitis animal model. Second, DCs are found within MS lesions and have been shown to be functionally abnormal in patients with MS. Lastly, therapeutics directed at DCs could potentially be engineered for treatment in MS and in fact may already be involved in the mechanisms of current immunomodulatory therapies.
UR - http://www.scopus.com/inward/record.url?scp=34249685435&partnerID=8YFLogxK
U2 - 10.1007/s11910-007-0037-z
DO - 10.1007/s11910-007-0037-z
M3 - Review article
C2 - 17488591
AN - SCOPUS:34249685435
SN - 1528-4042
VL - 7
SP - 245
EP - 252
JO - Current Neurology and Neuroscience Reports
JF - Current Neurology and Neuroscience Reports
IS - 3
ER -